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KeyLift™

FDA UDI

Class I (US FDA UDI)

by Flospine

Identity

Trade Name
KeyLift™ FDA UDI
Generic Name
Bone file/rasp, manual, reusable FDA UDI
Device Name
8mm Rasp Trial FDA UDI
Model / Reference
KeyLift™ FDA UDI
Description
8mm Rasp Trial FDA UDI

Identifiers

Catalog Number
07-7000-004 FDA UDI
Primary DI / UDI-DI
B1830770000040 FDA UDI
FDA Product Code
HTR FDA UDI
GMDN Term
Bone file/rasp, manual, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 8 Millimeter FDA UDI

Category: Bone file/rasp, manual, reusable

KeyLift™ by Flospine — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone file/rasp, manual, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flospine

Sources (1)

  • FDA UDI 60509444-82d8-4df6-abbb-049c7e4b821e 36 fields · synced May 30, 2026